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Translesion synthesis across O6-alkylguanine DNA adducts by recombinant human DNA polymerases

Translesion synthesis across O6-alkylguanine DNA adducts by recombinant human DNA polymerases
Choi J.-Y.Chowdhury G.Zang H.Angel K.C.Vu C.C.Peterson L.A.Guengerich F.P.
Ewha Authors
Issue Date
Journal Title
Journal of Biological Chemistry
0021-9258JCR Link
Journal of Biological Chemistry vol. 281, no. 50, pp. 38244 - 38256
Document Type
Previous studies have shown that replicative bacterial and viral DNA polymerases are able to bypass the mutagenic lesions O6-methyl and -benzyl (Bz) G. Recombinant human polymerase (pol) δ also copied past these two lesions but was totally blocked by O6-[4-oxo-4-(3-pyridyl) butyl] (Pob)G, an important mutagenic lesion formed following metabolic activation of the tobacco-specific carcinogen 4-(methylnitrosamino)-1-(3- pyridyl)-1-butanone. The human translesion pols ι and κ produced mainly only 1-base incorporation opposite O6-MeG and O 6-BzG and had very low activity in copying O6-PobG. Human pol η copied past all three adducts. Steady-state kinetic analysis showed similar efficiencies of insertion opposite the O6-alkylG adducts for dCTP and dTTP with pol η and κ; pol ι showed a strong preference for dTTP. pol η, ι, and κ showed pre-steady-state kinetic bursts for dCTP incorporation opposite G and O6-MeG but little, if any, for O6-BzG or O6-PobG. Analysis of the pol η O 6-PobG products indicated that the insertion of G was opposite the base (C) 5′ of the adduct, but this product was not extended. Mass spectrometry analysis of all of the pol η primer extension products indicated multiple components, mainly with C or T inserted opposite O 6-alkylG but with no deletions in the cases of O6-MeG and O6-PobG. With pol η and O6-BzG, products were also obtained with -1 and -2 deletions and also with A inserted (opposite O 6-BzG). The results with pol η may be relevant to some mutations previously reported with O6-alkylG adducts in mammalian cells. © 2006 by The American Society for Biochemistry and Molecular Biology, Inc.
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